Actively Recruiting
Taping and PMR Effects in Primary Dysmenorrhea
Led by Riphah International University · Updated on 2025-01-07
30
Participants Needed
1
Research Sites
58 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study is randomized controlled trial,The study conducted in two groups. Group A has given the kinesiology taping on the lower abdomen and back for 1-3 days with progressive muscle relaxation technique for 10-20 minutes and a baseline treatment hot pack at a time twice a day from the start of menstruation and Group B has receive the kinesiology taping on the lower abdomen and baseline treatment hot pack without progressive muscle relaxation technique for 1-3 days. The total treatment duration will be 6 weeks. The rationale of this study is to provide empirical evidence regarding the efficacy and safety of kinesiology taping and progressive muscle relaxation. By investigating the potential benefits of this intervention, healthcare professionals can make informed decisions about incorporating K-taping and PMR in primary dysmenorhea. Focusing on the impact of kinesiology taping and progressive muscle relaxation on pain,anxiety, and body awareness aligns with a patient-centered approach to care. The goal is not only to reduce symptoms but also to enhance overall well-being and functional capacity
CONDITIONS
Official Title
Taping and PMR Effects in Primary Dysmenorrhea
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged between 18 and 25 years
- Unmarried female
- Menstrual pain score of 4 or higher on the Visual Analog Scale during menstrual cycle
- Moderate menstrual pain as measured by WaLLID score
You will not qualify if you...
- Low back pain due to other causes, skin infection, sensitive skin, or allergy to kinesiology tape
- Polycystic ovary disease (PCOD), uterine or ovarian tumor
- Acute or chronic pelvic conditions such as pelvic inflammatory disease (PID), endometriosis
- Spinal pathology or deformity
- Endometrial polyp, pelvic infection, use of intrauterine device, or venous congestion in internal genital organs
- Current use of analgesics
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ghurki hospital
Lahore, Punjab Province, Pakistan, 54000
Actively Recruiting
Research Team
I
imran NA amjad, PhD
CONTACT
I
Iqra Abdul ghafoor, PPDPT
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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